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Merck Manufacturing Jobs in Raleigh, NC (NOW HIRING)

Keep current on cGMP, regulatory, and quality requirements impacting FDBN manufacturing and client guidance. Minimum Requirements * Bachelor's or Master's degree in a relevant field (sciences ...

New

By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof. We're ...

New

Senior Specialist, Operations

Durham, NC · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

As part of our company's Vaccine Manufacturing Organization, the Durham team is seeking a highly ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

Minimum of six (6) years of Process Engineering, Manufacturing, Technical support group or equivalent. * Bachelor's Degree (or Master's) in Mechanical, Chemical or Electrical Engineering or very ...

Senior Employee Relations Partner

Holly Springs, NC · On-site

$80 - $100/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill‑finish, and packaging under one roof. We're ...

Global CDMO Compliance Leader

Morrisville, NC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... and manufacturing organization (CDMO) for biologics, vaccines and advanced therapies. Reporting to the VP, Chief Compliance Officer of FUJIFILM Holdings America Corporation, this individual will ...

New

Global CDMO Compliance Officer

Morrisville, NC · On-site

$220 - $240/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... and manufacturing organization (CDMO) for biologics, vaccines and advanced therapies. Reporting to the VP, Chief Compliance Officer of FUJIFILM Holdings America Corporation, this individual will ...

New

Showing results 21-40

Merck Manufacturing information

See Raleigh, NC salary details

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How much do merck manufacturing jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for merck manufacturing in Raleigh, NC is $24.25, according to ZipRecruiter salary data. Most workers in this role earn between $19.62 and $28.03 per hour, depending on experience, location, and employer.

What is Merck Manufacturing?

Merck Manufacturing refers to the division of Merck & Co., Inc. responsible for the production and supply of medicines, vaccines, and other health products. This team manages the end-to-end manufacturing process, ensuring that products are made safely, efficiently, and to the highest quality standards. Merck Manufacturing includes roles in process development, quality assurance, supply chain management, and operations, supporting global healthcare needs. Their work is essential to delivering Merck's products to patients around the world.

What are the key skills and qualifications needed to thrive as a Merck Manufacturing professional?

To thrive in Merck Manufacturing, you need a strong background in life sciences or engineering, experience in GMP-regulated environments, and often a relevant degree such as chemical engineering, biology, or pharmaceutical sciences. Familiarity with manufacturing execution systems (MES), quality management software, and regulatory compliance certifications like Six Sigma or Lean are often required. Attention to detail, problem-solving abilities, and teamwork are essential soft skills to excel in this role. These skills ensure production quality, regulatory compliance, and efficient collaboration in delivering safe and effective pharmaceuticals.

What are some common challenges faced by professionals working in Merck Manufacturing, and how can they be addressed?

One common challenge in Merck Manufacturing is maintaining high quality and compliance standards while meeting production targets. Employees often need to adapt quickly to evolving regulatory requirements and new technologies. Effective communication and collaboration with cross-functional teams, such as quality assurance and engineering, are essential for overcoming these challenges. Additionally, Merck provides ongoing training and resources to help manufacturing professionals stay up-to-date and succeed in their roles.

What is the difference between Merck Manufacturing vs Merck Quality Control?

AspectMerck ManufacturingMerck Quality Control
Primary RoleOversees production processes, equipment, and manufacturing operationsEnsures product quality through testing, inspection, and validation
Required CertificationsManufacturing certifications, GMP trainingQuality assurance certifications, GMP training
Work EnvironmentFactories, production lines, manufacturing plantsLaboratories, testing facilities, quality labs
Industry UsageUsed in pharmaceutical manufacturing settingsUsed in quality assurance and control departments

Merck Manufacturing focuses on the production and assembly of pharmaceutical products, ensuring manufacturing efficiency and compliance. In contrast, Merck Quality Control emphasizes testing and verifying product quality to meet safety standards. Both roles are essential in the pharmaceutical industry and often work closely to ensure high-quality products reach consumers.

What job categories do people searching Merck Manufacturing jobs in Raleigh, NC look for?

The top searched job categories for Merck Manufacturing jobs in Raleigh, NC are:

Infographic showing various Merck Manufacturing job openings in Raleigh, NC as of August 2026, with employment types broken down into 88% Full Time, 6% Part Time, 3% Contract, and 3% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $50,441 per year, or $24.3 per hour.

Automation Engineer 3, DSM Upstream

Merck & Co.

Holly Springs, NC • On-site

$80 - $100/hr

Other

Posted 2 days ago

New


Merck rating

8.0

Company rating: 8.0 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

43rd of 86 rated pharmaceutical


Job description

Position Overview

The Automation Engineer 3, DSM Upstream, will provide support to the Drug Substance Manufacturing (DSM) facility using DeltaV. This includes implementing changes to the Automation systems, updating design documents, executing tests, troubleshooting events, and providing automation on-call support. This role focuses on supporting the delivery of DeltaV logic for Upstream process areas, including Inoculum Lab, Media Preparation, Seed Culture, Large Scale Bioreactors, and Harvest.

What You'll Do
  • Perform Automation activities, such as code configuration, document development, and test execution using DeltaV
  • Delivers accurate and on-time Automation work
  • Creates standard code utilizing simple control strategies
  • Assists with developing (generating, reviewing, maintaining) various specification documents (e.g., user requirements specification (URS), functional specification (FS), design qualification (DQ), etc.)
  • Assists with developing (generating, reviewing, maintaining) various test protocols and functional testing documents (e.g., installation qualification (IQ), operational qualification (OQ), etc.)
  • Assists with developing various test protocols and executes functional testing for documents (e.g.,
  • Serves as on-call support for Automation inquiries and troubleshooting
  • Collaborates with other departments, such as Manufacturing, Maintenance, and Validation
  • Other duties, as assigned
Knowledge and Skills
  • Effective communication, both written and oral
  • Basic problem-solving skills
  • Ability to present information to others
  • Ability to apply knowledge of Automation subject areas
Basic Requirements
  • Bachelor's degree in Chemical, Electrical, or Mechanical Engineering or other relevant field
  • 5 years of Automation, Instrumentation & Controls, or other relevant technical experience
  • DeltaV automation experience is required
  • Preferred: 6+ year of Automation experience
Working Conditions & Physical Requirements
  • Ability to discern audible cues.
  • Ability to stand for prolonged periods of time 30 minutes
  • Ability to sit for prolonged periods of time 240 minutes
  • Ability to conduct activities using repetitive motions that include wrists, hands, and/or fingers.
  • Ability to conduct work that includes moving objects up to 33 pounds.
EEO Information

Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national or social origin, disability, veteran status, etc.

ADA Information

If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBN_PNC@fujifilm.com).

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